Partial DiGeorge syndrome in two patients with a 10p rearrangement

Clinical Genetics

Volumn 55, Issue 4, 1999, Pages 269-276

  Van Esch, Hilde ^a   Groenen, Peter ^a   Daw, Sarah ^b   Poffyn, Ann ^c   Holvoet, Maureen ^d   Scambler, Peter ^b   Fryns, Jean Pierre ^d   Van de Ven, Wim ^a   Devriendt, Koen ^d,e  

^a DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c MPI H Hart   (Belgium)

^d UNIVERSITY OF LEUVEN   (Belgium)

^e CENTER FOR HUMAN GENETICS   (Belgium)

Author keywords

Chromosome 10p; DiGeorge syndrome; Exostoses; Translocation

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; CHROMOSOME 10P; CHROMOSOME 8; CHROMOSOME DELETION; CHROMOSOME INSERTION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; DIGEORGE SYNDROME; HUMAN; KARYOTYPE; PRIORITY JOURNAL;

CHILD; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 8; DEVELOPMENTAL DISABILITIES; DIGEORGE SYNDROME; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; TRANSLOCATION, GENETIC;

EID: 0033005166     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.1999.550410.x     Document Type: Article

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